Allele Registry

Canonical Allele Identifier: PA2825310915

Gene: NCDN HGNC NCBI

ClinVar Variation Id: 2434074

HGVS (amino-acid)	Matching Registered Transcripts
NP_001014839.1:p.Phe494Leu	CA339346376 NM_001014839.1:c.1480T>C CA339346387 NM_001014839.1:c.1482C>A CA339346389 NM_001014839.1:c.1482C>G